Evolution of Albumin on AOA1 Patients Supplemented With Coenzyme Q10

Ataxia with ocular apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia. Patients' phenotype associates early onset cerebellar ataxia, oculomotor apraxia, neuropathy and often intellectual disability, hypoalbuminaemia and hypercholesterolemia.

APTX gene mutations responsible for AOA1 disease were identified in a family previously reported with ataxia and Coenzyme Q10 deficiency. Therefore we measured muscle Coenzyme Q10 in six patients AOA1 and found decreased levels in five. Hypercholesterolaemia and low albumin levels represent hallmarks of the disease.

We thus propose therapeutic trial with Coenzyme Q10 in AOA1 patients, by using albumin evolution as primary endpoint.

Moreover several secondary endpoints will be performed:

• clinical examination (SARA scale)
• quantitative assessments of the ataxia (with the calculation of the Composite Cerebellar Functional Severity CCFS)
• biological criteria (prealbumin, cholesterol, alphafoetoprotein, blood count, hepatic checkup)
• oculographic examination.

The study is a multicentric randomised placebo controlled trial with two-year follow-up:

• during the first year, one group will be supplemented with Coenzyme Q10 while the other group will receive a placebo;
• during the second year, all patients will be supplemented with Coenzyme Q10 in order to assess long term safety and tolerance of the treatment.

Inclusion criteria

• 1. Diagnosis of ataxia with oculomotor apraxia type I (AOA1) confirmed by genetic molecular analysis
• 2. Age ≥ 18 years
• 3. Hypoalbuminemia
• 4. Efficient contraception for women of childbearing potential (with pregnancy test during each visit)
• 5. Signature of the written informed consent form
• 6. Presence of a support person (for patient with cognitive disorders)

Exclusion criteria

• 1. Hypersensitivity to one of the excipients (glycerin, ethanol, lecithin)
• 2. Absence of hypoalbuminemia
• 3. During the 2 months before inclusion :

• Use of CoQ10
• Treatment with antioxidants (vitamin C) and statins
• Use of drugs affecting mitochondrial activity
• Anti-cholesterol, thyroid hormones, anti-arrhythmic compounds, warfarin, metformin or clozapine
• 4. Treatment with vitamin E, calcium, magnesium and/or other vitamins with a concentration superior to 149 UI during more than 3 months before inclusion
• 5. Use of drugs interfering with catacholamine metabolism (reserpine, amphetamine, or inhibitors of the monoamine oxidase A, methylphenidate, cinnarizine) during the month before inclusion
• 6. Non balanced treatment with anxiolytics, hypnotics, tranquillizers and/or antidepressants during the month before inclusion
• 7. Hypothyroidism with thyroxin use
• 8. Epilepsy
• 9. Psychotic disorders
• 10. Pregnancy or lactation period
• 11. Woman of childbearing potential without efficient contraception
• 12. Participant to other therapeutic studies during the month before inclusion
• 13. Inability to receive a clear information on the research
• 14. Inability to participate to the totality of the study
• 15. Non affiliation to social security (beneficiary or assignee)
• 16. Refusal of signing the consent form